Chantal Tallaksen

Professor emeritus - Nevrologisk avdeling
Bilde av Chantal Tallaksen
English version of this page
Telefon +47 22868877
Mobiltelefon Kontornr: 22118644
Brukernavn
Besøksadresse 2.etg. Bygg 20 A Ullevål

Faglig bakgrunn

Tidligere erfaring fra indremedisin, doktorgrad i "thiamin og alkohol", som førte meg til nevrologi. Arbeidet på nevrologisk avdeling OUS siden 1989, først RH, fra 2002 avdeling Ullevål, med 4 år på Salpêtrière sykehus (Paris, Frankrike) inimellom. Bygget opp kompetanse for 1.  nevrodegenerative lidelser, primært monogenetiske tilstander, spesielt ataksier og spastisk parapareser , 2. myasthenia gravis.

Erfaring: fra undervisning (tidligere universitetsstipendiat, nå professor II stilling), kurs i nevrogenetikk, platform for nevrogenetisk forskning, vært med i VIRUUS, leder av forskningsgruppe I klinikken.

Forskningsområder:

- myasthenia gravis (deltatt I 2 europeiske prosjekter siden 2002, med to stipendiater). Sett på epidemiologiske aspekter, og vært på jakt etter kliniske, immunologiske  og genetiske markører. Mål er bade bedring av behandling for alle typer myasthenia gravis, og bedring av livskvalitet.

- nevrodegenerative lidelser: primært arvelige typer, dog er ofte sporadiske med. Konsentrert meg om spastisk paraparese og ataksier for egne prosjekter (4 stipendiater), er med flere europeiske nettverk og internasjonale samarbeids studier.

Ultimate goal: var å etablere en nasjonal kompetansesenter for  monogenetiske nevrodegenerative lidelser I Norge.

Publikasjoner

  • Hikmat, Omar; Naess, Karin; Engvall, Martin; Klingenberg, Claus; Rasmussen, Magnhild; Tallaksen, Chantal; Brodtkorb, Eylert; Østergaard, Elsebet; de Coo, Irenaeus F.M.; Pias-Peleteiro, Leticia; Isohanni, Pirjo; Uusimaa, Johanna; Darin, Niklas; Rahman, Shamima & Bindoff, Laurence (2020). Simplifying the clinical classification of polymerase gamma (POLG) disease based on age of onset; studies using a cohort of 155 cases. Journal of Inherited Metabolic Disease.  ISSN 0141-8955.  43(4), s 726- 736 . doi: 10.1002/jimd.12211 Fulltekst i vitenarkiv.
  • Lipka, Alexander F.; Boldingh, Marion; van Zwet, Erik W.; Schreurs, Marco W.J; Kuks, Jan B.M.; Tallaksen, Chantal; Titulaer, Maarten J. & Verschuuren, Jan J.G.M. (2019). Long‐term follow‐up, quality of life, and survival of patients with Lambert‐Eaton myasthenic syndrome. Neurology.  ISSN 0028-3878.  94(5), s e511- e520 . doi: 10.1212/WNL.0000000000008747
  • Rydning, Siri Lynne; Koht, Jeanette; Sheng, Ying; Sowa, Piotr; Hjorthaug, Hanne Sagsveen; Wedding, Iselin Marie; ERICHSEN, ANNE KJERSTI; Hynås, Inger Anette; Backe, Paul Hoff; Tallaksen, Chantal; Vigeland, Magnus Dehli & Selmer, Kaja Kristine (2019). Biallelic POLR3A variants confirmed as a frequent cause of hereditary ataxia and spastic paraparesis. Brain.  ISSN 0006-8950.  142:e12(4), s 1- 5 . doi: 10.1093/brain/awz041 Fulltekst i vitenarkiv.
  • Stenshorne, Ida; Rasmussen, Magnhild; Salvanos, Panagiotis; Tallaksen, Chantal; Bindoff, Laurence & Koht, Jeanette (2019). Fever-related ataxia: A case report of CAPOS syndrome. Cerebellum & ataxias.  ISSN 2053-8871.  6:2, s 1- 5 . doi: 10.1186/s40673-019-0096-3 Fulltekst i vitenarkiv.
  • Arntzen, Kjell Arne; Høyer, Helle; Ørstavik, Kristin; Tallaksen, Chantal; Vedeler, Christian A.; Østern, Rune André Helland; Nebuchennykh, Maria; Braathen, Geir Julius & Fagerheim, Toril (2018). Charcot-Marie-Tooth disease type 4C in Norway: Clinical characteristics, mutation spectrum and minimum prevalence. Neuromuscular Disorders.  ISSN 0960-8966.  28(8), s 639- 645 . doi: 10.1016/j.nmd.2018.06.004
  • Coutelier, Marie; Hammer, Monia B.; Stevanin, Giovanni; Monin, Marie-Lorraine; Davoine, Claire-Sophie; Mochel, Fanny; Labauge, Pierre; Ewenczyk, Claire; Ding, Jinhui; Gibbs, J Raphael; Hannequin, Didier; Melki, Judith; Toutain, Annick; Laugel, Vincent; Forlani, Sylvie; Charles, Perrine; Broussolle, Emmanuel; Thobois, Stéphane; Afenjar, Alexandra; Anheim, Mathieu; Calvas, Patrick; Castelnovo, Giovanni; de Broucker, Thomas; Vidailhet, Marie; Moulignier, Antoine; Ghnassia, Robert T.; Tallaksen, Chantal; Mignot, Cyril; Goizet, Cyril; Le Ber, Isabelle; Ollagnon-Roman, Elisabeth; Pouget, Jean; Brice, Alexis; Singleton, Andrew & Durr, Alexandra (2018). Efficacy of exome-targeted capture sequencing to detect mutations in known cerebellar ataxia genes. JAMA Neurology.  ISSN 2168-6149.  75(5), s 591- 599 . doi: 10.1001/jamaneurol.2017.5121
  • Hikmat, Omar; Naess, Karin; Engvall, Martin; Klingenberg, Claus; Rasmussen, Magnhild; Tallaksen, Chantal; Brodtkorb, Eylert; Fiskerstrand, Torunn; Isohanni, Pirjo; Uusimaa, Johanna; Darin, Niklas; Rahman, Shamima & Bindoff, Laurence (2018). Elevated cerebrospinal fluid protein in POLG-related epilepsy: Diagnostic and prognostic implications. Epilepsia.  ISSN 0013-9580.  59(8), s 1595- 1602 . doi: 10.1111/epi.14459
  • Parodi, Livia; Fenu, Silvia; Barbier, Mathieu; Banneau, Guillaume; Duyckaerts, Charles; du Montcel, Sophie Tezenas; Monin, Marie-Lorraine; Said, Samia Ait; Guegan, Justine; Tallaksen, Chantal; Sablonniere, Bertrand; Brice, Alexis; Stevanin, Giovanni; Depienne, Christel & Durr, Alexandra (2018). Spastic paraplegia due to SPAST mutations is modified by the underlying mutation and sex. Brain.  ISSN 0006-8950.  141(12), s 3331- 3342 . doi: 10.1093/brain/awy285
  • Rydning, Siri Lynne; Dudesek, Ales; Rimmele, Florian; Funke, Claudia; Krüger, Stefanie; Biskup, Saskia; Vigeland, Magnus Dehli; Hjorthaug, Hanne Sagsveen; Sejersted, Yngve; Tallaksen, Chantal; Selmer, Kaja Kristine & Kamm, Christoph (2018). A novel heterozygous variant in ERLIN2 causes autosomal dominant pure hereditary spastic paraplegia. European Journal of Neurology.  ISSN 1351-5101.  25(7), s 943- 948 . doi: 10.1111/ene.13625
  • Sjaastad, Ottar; Blau, Nenad; Rydning, Siri Lynne; Peters, Verena; Rødningen, Olaug Kristin; Stray-Pedersen, Asbjørg; Krossnes, Bård Kronen; Tallaksen, Chantal & Koht, Jeanette (2018). Homocarnosinosis: A historical update and findings in the SPG11 gene. Acta Neurologica Scandinavica.  ISSN 0001-6314.  138(3), s 245- 250 . doi: 10.1111/ane.12949
  • Boldingh, Marion; Maniaol, Angelina; Brunborg, Cathrine; Dekker, Luuk; Lipka, Alexander F.; Niks, Erik Harmen; Verschuuren, Jan & Tallaksen, Chantal (2017). Prevalence and clinical aspects of immigrants with myasthenia gravis in northern Europe. Muscle and Nerve.  ISSN 0148-639X.  55(6), s 819- 827 . doi: 10.1002/mus.25408
  • Giordano, Ilaria; Harmuth, Florian; Jacobi, Heike; Paap, Brigitte; Vielhaber, Stefan; MacHts, Judith; Schols, Ludger; Synofzik, Matthis; Sturm, Marc; Tallaksen, Chantal; Wedding, Iselin Marie; Boesch, Sylvia; Eigentler, Andreas; Van De Warrenburg, Bart; Van Gaalen, Judith; Kamm, Christoph; Dudesek, Ales; Kang, Jun-Suk; Timmann, Dagmar; Silvestri, Gabriella; Masciullo, Marcella; Klopstock, Thomas; Neuhofer, Christiane; Ganos, Christos; Filla, Alessandro; Bauer, Peter; Tezenas Du Montcel, Sophie & Klockgether, Thomas (2017). Clinical and genetic characteristics of sporadic adult-onset degenerative ataxia. Neurology.  ISSN 0028-3878.  89(10), s 1043- 1049 . doi: 10.1212/WNL.0000000000004311
  • Hikmat, Omar; Tzoulis, Charalampos; Klingenberg, Claus; Rasmussen, Magnhild; Tallaksen, Chantal; Brodtkorb, Eylert; Fiskerstrand, Torunn; McFarland, Robert; Rahman, Shamima & Bindoff, Laurence (2017). The presence of anaemia negatively influences survival in patients with POLG disease. Journal of Inherited Metabolic Disease.  ISSN 0141-8955.  40(6), s 861- 866 . doi: 10.1007/s10545-017-0084-9
  • Iqbal, Zafar; Rydning, Siri Lynne; Wedding, Iselin Marie; Koht, Jeanette; Pihlstrøm, Lasse; Rengmark, Aina Sylvia Haugen; Henriksen, Sandra Pilar; Tallaksen, Chantal & Toft, Harald Mathias Strøm (2017). Targeted high throughput sequencing in hereditary ataxia and spastic paraplegia. PLOS ONE.  ISSN 1932-6203.  12:e0174667(3), s 1- 19 . doi: 10.1371/journal.pone.0174667 Fulltekst i vitenarkiv.
  • Rydning, Siri Lynne; Backe, Paul Hoff; Sousa, Mirta; Iqbal, Zafar; Øye, Ane-Marte; Sheng, Ying; Yang, Mingyi; Lin, Xiaolin; Slupphaug, Geir; Nordenmark, Tonje Haug; Vigeland, Magnus Dehli; Bjørås, Magnar; Tallaksen, Chantal & Selmer, Kaja Kristine (2017). Novel UCHL1 mutations reveal new insights into ubiquitin processing. Human Molecular Genetics.  ISSN 0964-6906.  26(6), s 1031- 1040 . doi: 10.1093/hmg/ddw391 Fulltekst i vitenarkiv.
  • Boldingh, Marion; Maniaol, Angelina; Brunborg, Cathrine; Weedon-Fekjær, Harald; Verschuuren, Jan J. G. M & Tallaksen, Chantal (2016). Increased risk for clinical onset of myasthenia gravis during the postpartum period. Neurology.  ISSN 0028-3878.  87(20), s 2139- 2145 . doi: 10.1212/WNL.0000000000003339
  • Horn, Morten Andreas; Müller, Karin Brigitte; Ferdinandusse, Sacha; Jørum, Ellen; Mellgren, Svein Ivar; Retterstøl, Lars; Wanders, Ronald J.A. & Tallaksen, Chantal (2016). Mild phenotype in an adult male with X‐linked adrenoleukodystrophy – case report. Clinical Case Reports.  ISSN 2050-0904.  4(2), s 177- 181 . doi: 10.1002/ccr3.434 Fulltekst i vitenarkiv.
  • Koht, Jeanette; Løstegaard, Sven Olav; Wedding, Iselin Marie; Vidailhet, Marie; Louha, Malek & Tallaksen, Chantal (2016). Benign hereditary chorea, not only chorea: a family case presentation. Cerebellum & ataxias.  ISSN 2053-8871.  3 . doi: 10.1186/s40673-016-0041-7
  • Rydning, Siri Lynne; Wedding, Iselin Marie; Koht, Jeanette; Chawla, Maninder Singh; Øye, Ane-Marte; Sheng, Ying; Vigeland, Magnus Dehli; Selmer, Kaja Kristine & Tallaksen, Chantal (2016). A founder mutation p.H701P identified as a major cause of SPG7 in Norway. European Journal of Neurology.  ISSN 1351-5101.  23(4), s 763- 771 . doi: 10.1111/ene.12937 Fulltekst i vitenarkiv. Vis sammendrag
  • Simonsen, Cecilia Smith; Celius, Elisabeth Gulowsen; Brunborg, Cathrine; Tallaksen, Chantal; Eriksen, Erik Fink; Holmøy, Trygve & Moen, Stine Marit (2016). Bone mineral density in patients with multiple sclerosis, hereditary ataxia or hereditary spastic paraplegia after at least 10 years of disease - a case control study. BMC Neurology.  ISSN 1471-2377.  16 . doi: 10.1186/s12883-016-0771-4
  • Stergiou, Christos; Lazaridis, Konstantinos; Zouvelou, Vasiliki; Tzartos, John; Mantegazza, Renato; Antozzi, Carlo; Andreetta, Francesca; Evoli, Amelia; Deymeer, Feza; Saruhan-Direskeneli, Güher; Durmuş, Hacer; Brenner, Talma; Vaknin, Adi; Berrih-Aknin, Sonia; Behin, Anthony; Sharshar, Tarek; De Baets, Marc H.; Losen, Mario; Martínez-Martínez, Pilar; Kleopa, Kleopas A.; Zamba-Papanicolaou, Eleni; Kyriakides, Theodoros; Kostera-Pruszczyk, Anna; Szczudlik, Piotr; Szyluk, Beata; Lavrnic, Dragana; Basta, Ivana; Peric, Sanja; Tallaksen, Chantal; Maniaol, Angelina; Gilhus, Nils Erik; Casasnovas Pons, Carlos; Pitha, Jan V.; Jakubíková, Michala; Hanisch, Frank; Bogomolovas, Julius; Labeit, Dietmar; Labeit, Sigfried Bernhard & Tzartos, Socrates J. (2016). Titin antibodies in "seronegative" myasthenia gravis - A new role for an old antigen. Journal of Neuroimmunology.  ISSN 0165-5728.  292, s 108- 115 . doi: 10.1016/j.jneuroim.2016.01.018
  • Boldingh, Marion Ingeborg; Dekker, Luuk; Maniaol, Angelina; Brunborg, Cathrine; Lipka, Alexander F.; Niks, Erik H.; Verschuuren, Jan J.G.M. & Tallaksen, Chantal (2015). An up-date on health-related quality of life in myasthenia gravis -results from population based cohorts. Health and Quality of Life Outcomes.  ISSN 1477-7525.  13:115 . doi: 10.1186/s12955-015-0298-1
  • Boldingh, Marion Ingeborg; Maniaol, Angelina; Brunborg, Cathrine; Dekker, Luuk; Heldal, Anne Taraldsen; Lipka, Alexander F.; Popperud, Trine Haug; Niks, Erik H.; Verschuuren, Jan J.G.M. & Tallaksen, Chantal (2015). Geographical distribution of myasthenia gravis in Northern Europe - Results from a population-based study from two countries. Neuroepidemiology.  ISSN 0251-5350.  44(4), s 221- 231 . doi: 10.1159/000431036
  • Coutelier, Marie; Goizet, Cyril; Durr, Alexandra; Habarou, Florence; Morais, Sara; Dionne-Laporte, Alexandre; Tao, Feifei; Konop, Juliette; Stoll, Marion; Charles, Perrine; Jacoupy, Maxime; Matusiak, Raphaël; Alonso, Isabel; Tallaksen, Chantal; Mairey, Mathilde; Kennerson, Marina; Gaussen, Marion; Schule, Rebecca; Janin, Maxime; Morice-Picard, Fanny; Durand, Christelle M.; Depienne, Christel; Calvas, Patrick; Coutinho, Paula; Saudubray, Jean-Marie; Rouleau, Guy; Brice, Alexis; Nicholson, Garth; Darios, Frédéric; Loureiro, José L.; Zuchner, Stephan; Ottolenghi, Chris; Mochel, Fanny & Stevanin, Giovanni (2015). Alteration of ornithine metabolism leads to dominant and recessive hereditary spastic paraplegia. Brain.  ISSN 0006-8950.  138(8), s 2191- 2205 . doi: 10.1093/brain/awv143
  • Tsonis, Anastasios I.; Zisimopoulou, Paraskevi; Lazaridis, Konstantinos N.; Tzartos, John; Matsigkou, Eirini; Zouvelou, Vasiliki; Mantegazza, Renato; Antozzi, Carlo; Andreetta, Francesca; Evoli, Amelia; Deymeer, Feza; Saruhan-Direskeneli, Güher; Durmuş, Hacer; Brenner, Talma; Vaknin-Dembinsky, Adi; Berrih-Aknin, Sonia; Behin, Anthony; Sharshar, Tarek; De Baets, Marc H.; Losen, Mario; Martínez-Martínez, Pilar; Kleopa, Kleopas A.; Zamba-Papanicolaou, Eleni; Kyriakides, Theodoros; Kostera-Pruszczyk, Anna; Szczudlik, Piotr; Szyluk, Beata; Lavrnic, Dragana; Basta, Ivana; Perić, Stojan; Tallaksen, Chantal; Maniaol, Angelina; Pons, Carlos Casasnovas; Pitha, Jan V.; Jakubíková, Michala; Hanisch, Frank & Tzartos, Socrates J. (2015). MuSK autoantibodies in myasthenia gravis detected by cell based assay - A multinational study. Journal of Neuroimmunology.  ISSN 0165-5728.  284, s 10- 17 . doi: 10.1016/j.jneuroim.2015.04.015
  • Wedding, Iselin Marie; Kroken, Mette; Henriksen, Sandra Pilar; Selmer, Kaja Kristine; Fiskerstrand, Torunn; Knappskog, Per; Berge, Tone & Tallaksen, Chantal (2015). Friedreich ataxia in Norway - An epidemiological, molecular and clinical study. Orphanet Journal of Rare Diseases.  ISSN 1750-1172.  10(1), s 1- 17 . doi: 10.1186/s13023-015-0328-4 Fulltekst i vitenarkiv. Vis sammendrag
  • Avidan, Nili; Panse, Rozen Le; Harbo, Hanne Flinstad; Bernasconi, Pia; Poulas, Konstantinos; Ginzburg, Elizabeta; Cavalcante, Paola; Colleoni, Lara; Baggi, Fulvio; Antozzi, Carlo; Truffault, Frederique; Horn-Saban, Shirley; Poschel, Simone; Zagoriti, Zoi; Maniaol, Angelina; Lie, Benedicte Alexandra; Bernard, Isabelle; Saoudi, Abdelhadi; Illes, Zsolt; Pons, Carlos Casasnovas; Melms, Arthur; Tzartos, Socrates; Willcox, Nicholas; Kostera-Pruszczyk, Anna; Tallaksen, Chantal; Mantegazza, Renato; Berrih-Aknin, S. & Miller, Ariel (2014). VAV1 and BAFF, via NFκB pathway, are genetic risk factors for myasthenia gravis. Annals of clinical and translational neurology.  ISSN 2328-9503.  1(5), s 329- 339 . doi: 10.1002/acn3.51
  • Heimdal, Ketil Riddervold; Sanchez Guixe, Monica; Aukrust, Ingvild; Bollerslev, Jens; Bruland, Ove; Jablonski, Greg; ERICHSEN, ANNE KJERSTI; Gude, Einar; Koht, Jeanette; Erdal, Sigrid; Fiskerstrand, Torunn; Haukanes, Bjørn Ivar; Boman, Helge; Bjørkhaug, Lise; Tallaksen, Chantal; Knappskog, Per & Johansson, Stefan (2014). STUB1 mutations in autosomal recessive ataxias - evidence for mutation-specific clinical heterogeneity. Orphanet Journal of Rare Diseases.  ISSN 1750-1172.  9:146 . doi: 10.1186/s13023-014-0146-0 Fulltekst i vitenarkiv.
  • Horn, Morten Andreas; Nilsen, Kristian Bernhard; Jørum, Ellen; Mellgren, Svein Ivar & Tallaksen, Chantal (2014). Small nerve fiber involvement is frequent in X-linked adrenoleukodystrophy. Neurology.  ISSN 0028-3878.  82(19), s 1678- 1683 . doi: 10.1212/WNL.0000000000000415
  • Koht, Jeanette; Rengmark, Aina Sylvia Haugen; Opladen, Thomas; Bjørnarå, Kari Anne; Selberg, Tore; Tallaksen, Chantal; Blau, N. & Toft, Mathias (2014). Clinical and genetic studies in a family with a novel mutation in the sepiapterin reductase gene. Acta Neurologica Scandinavica.  ISSN 0001-6314.  129(198), s 7- 12 . doi: 10.1111/ane.12230
  • Wedding, Iselin Marie; Koht, Jeanette; Tran, Gia Tuong Thi; Misceo, Doriana; Selmer, Kaja Kristine; Holmgren, Asbjørn; Frengen, Eirik; Bindoff, Laurence; Tallaksen, Chantal & Tzoulis, Charalampos (2014). Spastic paraplegia type 7 is associated with multiple mitochondrial DNA deletions. PLOS ONE.  ISSN 1932-6203.  9(1) . doi: 10.1371/journal.pone.0086340 Fulltekst i vitenarkiv.
  • Zisimopoulou, P.; Evangelakou, P.; Tzartos, J.; Lazaridis, K.; Zouvelou, V.; Mantegazza, Renato; Antozzi, C.; Andreetta, F.; Evoli, A; Deymeer, F.; Saruhan-Direskeneli, G; Durmus, H.; Brenner, T.; Vaknin, A.; Berrih-Aknin, S.; Cuvelier, M. Frenkian; Stojkovic, T.; DeBaets, M.; Losen, M.; Martinez-Martinez, P.; Kleopa, K.A.; Zamba-Papanicolaou, E.; Kyriakides, Theodoros; Kostera-Pruszczyk, A.; Szczudlik, P.; Szyluk, B.; Lavrnic, D.; Basta, I.; Peric, S.; Tallaksen, Chantal; Maniaol, Angelina & Tzartos, S.J (2014). A comprehensive analysis of the epidemiology and clinical characteristics of anti-LRP4 in myasthenia gravis. Journal of Autoimmunity.  ISSN 0896-8411.  52, s 139- 145 . doi: 10.1016/j.jaut.2013.12.004
  • Horn, Morten Andreas; Erichsen, Martina Moter; Wolff, Anette Susanne Bøe; Månsson, Jan-Eric; Husebye, Eystein Sverre; Tallaksen, Chantal & Skjeldal, Ola (2013). Screening for X-linked adrenoleukodystrophy among adult men with Addison's disease. Clinical Endocrinology.  ISSN 0300-0664.  79(3), s 316- 320 . doi: 10.1111/cen.12159
  • Horn, Morten Andreas; Retterstøl, Lars; Abdelnoor, Michael; Skjeldal, Ola & Tallaksen, Chantal (2013). Adrenoleukodystrophy in Norway: High Rate of De Novo Mutations and Age-Dependent Penetrance. Pediatric Neurology.  ISSN 0887-8994.  48(3), s 212- 219 . doi: 10.1016/j.pediatrneurol.2012.12.007
  • Maniaol, Angelina; Boldingh, Marion Ingeborg; Brunborg, Cathrine; Harbo, Hanne Flinstad & Tallaksen, Chantal (2013). Smoking and socio-economic status may affect myasthenia gravis. European Journal of Neurology.  ISSN 1351-5101.  20(3), s 453- 460 . doi: 10.1111/j.1468-1331.2012.03843.x
  • Sumathipala, Dulika S.; Abeysekera, Gayan S.; Jayasekara, Rohan W.; Tallaksen, Chantal & Dissanayake, Vajira H.W (2013). Autosomal dominant hereditary ataxia in Sri Lanka. BMC Neurology.  ISSN 1471-2377.  13 . doi: 10.1186/1471-2377-13-39
  • Wedding, Iselin Marie; Koht, Jeanette; Dietrichs, Espen; Landrø, Nils Inge & Tallaksen, Chantal (2013). Cognition is only minimally impaired in Spinocerebellar ataxia type 14 (SCA14): a neuropsychological study of ten Norwegian subjects compared to intrafamilial controls and population norm. BMC Neurology.  ISSN 1471-2377.  13:186 . doi: 10.1186/1471-2377-13-186 Fulltekst i vitenarkiv.
  • Gregersen, Peter K.; Kosoy, Roman; Lee, Annette T.; Lamb, Janine; Sussman, Jon; McKee, David; Simpfendorfer, Kim R.; Pirskanen-Matell, Ritva; Piehl, Frederik; Pan-Hammarstrom, Qiang; Verschuuren, Jan J. G. M; Titulaer, Maarten J.; Niks, Erik N.; Marx, Alexander; Ströbel, Philipp; Tackenberg, Björn; Pütz, Michael; Maniaol, Angelina; Elsais, Ahmed; Tallaksen, Chantal; Harbo, Hanne Flinstad; Lie, Benedicte Alexandra; Raychaudhuri, Soumya; de Bakker, Paul L. W.; Melms, Arthur; Garchon, Henri-Jean; Willcox, Nicholas; Hammarstrom, Lennart & Seldin, Michael F. (2012). Risk for Myasthenia Gravis Maps to a 151Pro!Ala Change in TNIP1 and to Human Leukocyte Antigen-B*08. Annals of Neurology.  ISSN 0364-5134.  72(6), s 927- 935 . doi: 10.1002/ana.23691
  • Koht, Jeanette; Stevanin, G; Durr, A; Mundwiller, E; Brice, A & Tallaksen, Chantal (2012). SCA14 in Norway, two families with autosomal dominant cerebellar ataxia and a novel mutation in the PRKCG gene. Acta Neurologica Scandinavica.  ISSN 0001-6314.  125(2), s 116- 122 . doi: 10.1111/j.1600-0404.2011.01504.x
  • Maniaol, Angelina; Elsais, Ahmed; Lorentzen, Åslaug Rudjord; Owe, Jone Furulund; Viken, Marte K; Sæther, Hanne Skarpodde; Flåm, Siri Tennebø; Bråthen, Geir; Kampman, Margitta Theodora; Midgard, Rune; Christensen, Marte; Rognerud, Anna Kaja; Kerty, Emilia; Gilhus, Nils Erik; Tallaksen, Chantal; Lie, Benedicte Alexandra & Harbo, Hanne Flinstad (2012). Late onset myasthenia gravis is associated with HLA DRB1*15:01 in the Norwegian population. PLOS ONE.  ISSN 1932-6203.  7(5) . doi: 10.1371/journal.pone.0036603 Fulltekst i vitenarkiv.
  • Alseth, Espen Homleid; Maniaol, Angelina; Elsais, Ahmed; Nakkestad, Hanne Linda; Tallaksen, Chantal; Gilhus, Nils Erik & Skeie, Geir Olve (2011). Investigation for RAPSN and DOK-7 mutations in a cohort of seronegative myasthenia gravis patients. Muscle and Nerve.  ISSN 0148-639X.  43(4), s 574- 577 . doi: 10.1002/mus.21919
  • Burgunder, Jean-Marc; Schöls, Ludger; Baets, Jonathan; Andersen, Peter Munch; Gasser, Thomas; Szolnoki, Zoltan; Fontaine, Bertrand; Van Broeckhoven, Christina; Di Donato, Stefano; De Jonghe, Peter; Lynch, Timothy; Mariotti, Caterina; Spinazzola, Antonella; Tabrizi, Sarah J.; Tallaksen, Chantal; Zeviani, Massimo; Harbo, Hanne Flinstad & Finsterer, Josef (2011). EFNS guidelines for the molecular diagnosis of neurogenetic disorders: motoneuron, peripheral nerve and muscle disorders. European Journal of Neurology.  ISSN 1351-5101.  18(2), s 207- E20 . doi: 10.1111/j.1468-1331.2010.03069.x
  • Holmøy, Trygve; Braaten, Øivind; Hynås, Inger Anette & Tallaksen, Chantal (2011). En ung kvinne som mistet kraften i ett bein. Tidsskrift for Den norske legeforening.  ISSN 0029-2001.  6, s 583- 586
  • Burgunder, J-M.; Finsterer, J.; Szolnoki, Z.; Fontaine, B.; Baets, J.; Van Broeckhoven, C.; Di Donato, S.; De Jonghe, P.; Lynch, T.; Mariotti, C.; Schöls, L.; Spinazzola, A.; Tabrizi, S. J.; Tallaksen, Chantal; Zeviani, M.; Harbo, Hanne Flinstad & Gasser, T. (2010). EFNS guidelines on the molecular diagnosis of channelopathies, epilepsies, migraine, stroke, and dementias. European Journal of Neurology.  ISSN 1351-5101.  17(5), s 641- 648 . doi: 10.1111/j.1468-1331.2010.02985.x
  • Burgunder, JM; Et al, More authors; Tallaksen, Chantal & Harbo, Hanne Flinstad (2010). EFNS guidelines for the molecular diagnosis of neurodegenerative disorders:motoneuron, peripheral nerve and muscle disorders. European Journal of Neurology.  ISSN 1351-5101.  18, s 207- 217 . doi: 10.1111/j.468-1331.2010.03069.x
  • Gasser, T; Finsterer, Josef; Baets, J; Van Broeckhoven, C; Di Donato, S; Fontaine, B; De Jonghe, P; Lossos, A; Lynch, T; Mariotti, C; Schols, L; Spinazzola, A; Szolnoki, Z; Tabrizi, SJ; Tallaksen, Chantal; Zeviani, M; Burgunder, JM & Harbo, Hanne Flinstad (2010). EFNS guidelines on the molecular diagnosis of ataxias and spastic paraplegias. European Journal of Neurology.  ISSN 1351-5101.  17(2), s 179- 188 . doi: 10.1111/j.1468-1331.2009.02873.x
  • Koht, Jeanette; Tallaksen, Chantal & ERICHSEN, ANNE KJERSTI (2010). Kapitell om ataksier og spastiske parapareser, I: Leif Gjerstad; Eirik Helseth & Terje Rootwelt (red.),  Nevrologi og nevrokirurgi. Fra barn til voksen. 5.utgave.  Forlaget Vett & Viten.  ISBN 978-82-412-0686-3.  Arvelige ataksier og spastiske parapareser.
  • Maniaol, Angelina; Brunborg, Cathrine & Tallaksen, Chantal (2010). Development and Validation of a Self-Administered Questionnaire for Myasthenia Gravis Patients. Neuroepidemiology.  ISSN 0251-5350.  34(4), s 253- 261 . doi: 10.1159/000297753
  • Schlipf, NA; Beetz, C; Schule, R; Stevanin, G; ERICHSEN, ANNE KJERSTI; Forlani, S; Zaros, C; Karle, K; Klebe, S; Klimpe, S; Durr, A; Otto, S; Tallaksen, Chantal; Riess, O.; Brice, Alexis.; Bauer, Peter & Schols, L (2010). A total of 220 patients with autosomal dominant spastic paraplegia do not display mutations in the SLC33A1 gene (SPG42). European Journal of Human Genetics.  ISSN 1018-4813.  18(9), s 1065- 1067 . doi: 10.1038/ejhg.2010.68
  • Yu-Wai-Man, Patrick; Griffiths, Philip G.; Gorman, Grainne S.; Lourenco, Charles Marques; Wright, Alan F.; Auer-Grumbach, Michaela; Toscano, Antonio; Musumeci, Olimpia; Valentino, Maria L.; Caporali, Leonardo; Lamperti, Constanza; Tallaksen, Chantal; Duffey, Paul; Miller, Jonathan L.; Whittaker, Roger Graham; Baker, Mark R.; Jackson, Malcolm J.; Clarke, Michael P.; Dhillon, Baljean; Czermin, Birgit; Stewart, Joanna D.; Hudson, Gavin; Reynier, Pascal; Bonneau, Dominique; Marques Jr., Wilson; Lenaers, Guy; McFarland, Robert; Taylor, Robert W.; Turnbull, Douglass M; Votruba, Marcela; Zeviani, Massimo; Carelli, Valerio; Bindoff, Laurence; Horvath, Rita; Amati-Bonneau, Patrizia & Chinnery, Patrick F. (2010). Multi-system neurological disease is common in patients with OPA1 mutations. Brain.  ISSN 0006-8950.  133, s 771- 786 . doi: 10.1093/brain/awq007
  • ERICHSEN, ANNE KJERSTI; Koht, Jeanette; Stray-Pedersen, Asbjørg; Abdelnoor, Michael & Tallaksen, Chantal (2009). Prevalence of hereditary ataxia and spastic paraplegia in southeast Norway: a population-based study. Brain.  ISSN 0006-8950.  132, s 1577- 1588 . doi: 10.1093/brain/awp056
  • ERICHSEN, ANNE KJERSTI; Server, A.; Landrø, Nils Inge; Sandvik, L & Tallaksen, Chantal (2009). Proton magnetic resonance spectroscopy and cognition in patients with spastin mutations. Journal of the Neurological Sciences.  ISSN 0022-510X.  277(1-2), s 124- 129 . doi: 10.1016/j.jns.2008.10.030
  • Koht, Jeanette Aimee; Bjornara, KA; Jørum, Ellen & Tallaksen, Chantal (2009). Ataxia with vitamin E deficiency in southeast Norway, case report. Acta Neurologica Scandinavica.  ISSN 0001-6314.  120, s 42- 45
  • Selmer, Kaja K.; Eriksson, AS; Brandal, K; Egeland, Thore; Tallaksen, C & Undlien, DE (2009). Parental SCN1A mutation mosaicism in familial Dravet syndrome. Clinical Genetics.  ISSN 0009-9163.  76(4), s 398- 403 . doi: 10.1111/j.1399-0004.2009.01208.x
  • Vevelstad, Merete Synnøve; Pettersen, S; Tallaksen, C & Brørs, Odd (2009). O-demethylation of codeine to morphine inhibited by low-dose levomepromazine. European Journal of Clinical Pharmacology.  ISSN 0031-6970.  65(8), s 795- 801 . doi: 10.1007/s00228-009-0640-9
  • Erichsen, AK; Stevanin, G; Denora, P; Brice, A & Tallaksen, Chantal (2008). SPG11 - the most common type of recessive spastic paraplegia in Norway?. Acta Neurologica Scandinavica.  ISSN 0001-6314.  117, s 46- 50
  • Tallaksen, Chantal (2008). Arvelige ataksier. Tidsskrift for Den norske legeforening.  ISSN 0029-2001.  128(17), s 1977- 1980
  • Erichsen, AK; Inderhaug, E; Mattingsdal, M; Eiklid, K & Tallaksen, Chantal (2007). Seven novel mutations and four exon deletions in a collection of Norwegian patients with SPG4 hereditary spastic paraplegia. European Journal of Neurology.  ISSN 1351-5101.  14, s 809- 814 . doi: 10.1111/j.1468-1331.2007.01861.x
  • Horn, Morten Andreas; van den Brink, D. M.; Wanders, R.J.A.; Duran, Marinus; Poll-The, B. T.; Tallaksen, Chantal; Stokke, Oddvar; Moser, H. & Skjeldal, Ola (2007). Phenotype of adult Refsum disease due to a defect in peroxin 7. Neurology.  ISSN 0028-3878.  68, s 698- 700 . doi: 10.1212/01.wnl.0000257903.51937.88 Vis sammendrag
  • Koht, Jeanette Aimee & Tallaksen, Chantal (2007). Cerebellar ataxia in the eastern and southern parts of Norway. Acta Neurologica Scandinavica.  ISSN 0001-6314.  115
  • Depienne, C; Tallaksen, Chantal; Lephav, JY; Bricka, B; Poea-Guvon, S; Fontaine, B; Labauge, P; Brice, A & Durr, A (2005). Spastin mutations are frequent in sporadic spastic paraparesis and their spectrum is different from the one observed in familial cases. Journal of Medical Genetics.  ISSN 0022-2593.
  • Dürr, A; Camuzat, A; Colin, E; Tallaksen, Chantal; Hannequin, D; Couthino, P; Fontaine, B; Rossi, A; Gil, R; Boggio, D; Ruberg, M; Stevanin, G & Brice, A (2004). Atlastin mutations are frequent in young onset autosomal dominant spastic paralegia. Archives of Neurology.  ISSN 0003-9942.  61, s 1867- 1873
  • Dürr, A & Tallaksen, Chantal (2004). SPG4 Hereditary Spastic Paraplegia. Gene Reviews : Gene Tests.
  • Tallaksen, Chantal & Dietrichs, Espen (2004). Genetikk ved bevegelsesforstyrrelser- spinocerebellære lidelser. Tidsskrift for Den norske legeforening.  ISSN 0029-2001.  17(124), s 2233- 2235
  • Tallaksen, Chantal; Guichart-Gomez, E; Verpillat, P; Hahn-Barma, V; Ruberg, M; Fontaine, B; Brice, A; Dubois, B & Dürr, A (2004). Subtle cognitive inpairment but no dementia in patients with spastin mutations. Archives of Neurology.  ISSN 0003-9942.  60, s 1113- 1118
  • Tallaksen, Chantal; Guichart-Gomez, E; Verpillat, P; Hahn-Barma, V; Ruberg, M; Fontaine, B; Brice, A; Dubois, B & Dürr, A (2004). Subtle, cognitive impairment but no dementia in patients with spastims mutations. Archives of Neurology.  ISSN 0003-9942.  60, s 1113- 1118
  • Tallaksen, Chantal; Skjeldal, OH & Gjerstad, L (2004). Spinocecerebellare degenerasjoner. In Nevrologi og Nevrokirurgi, Vett & Viten AS.  (3), s 423- 430
  • Dietrichs, Espen & Tallaksen, Chantal (2004). Genetikk ved bevegelsesforstyrrelser - dystoni, tremor og chorea. Tidsskrift for Den norske legeforening.  ISSN 0029-2001.  (Årg. 124, nr 17), s 2236-2237
  • Tallaksen, Chantal (2003). Subtle cognitive impairment but no dementia in patients with spastin mutations. Archives of Neurology.  ISSN 0003-9942.  60, s 1113- 1118
  • Tallaksen, Chantal; Sande, Sverre Arne; Bøhmer, Thomas; Bell, Helge & Karlsen, Jan (1993). Kinetics of thiamin phosphate esters in human blood, plasma and urine after 50 mg intravenously or orally. European Journal of Clinical Pharmacology.  ISSN 0031-6970.  44, s 73- 78

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  • Arntzen, Kjell Arne; Høyer, Helle; Ørstavik, Kristin; Tallaksen, Chantal; Vedeler, Christian A.; Østern, Rune André Helland; Nebuchennykh, Maria; Braathen, Geir J. & Fagerheim, Toril (2018). Clinical characteristics, minimum prevalence and spectrum of SH3TC2 mutations in Norway.
  • Samuelsson, Kristin; Radovic, Ana; Press, Rayomond; Auranen, Mari; Ylikallio, Emil; Tyynismaa, Henna; Kärppä, Mikko; Veteläinen, Matilda; Peltola, Niina; Mellgren, Svein Ivar; Mygland, Åse; Tallaksen, Chantal; Andersen, Henning; Terkelsen, Astrid Juhl; Fontain, Freja & Hietaharju, Aki (2018). Screening for Fabry disease and Hereditary ATTR amyloidosis in idiopathic small-fiber and mixed neuropathy. Muscle and Nerve.  ISSN 0148-639X.  59(3), s 354- 357 . doi: 10.1002/mus.26348
  • Hikmat, Omar; Tzoulis, Charalampos; Klingenberg, Claus; Rasmussen, Magnhild; Tallaksen, Chantal; Brodtkorb, Eylert; Fiskerstrand, Torunn; McFarland, Robert; Rahman, Shamima & Bindoff, Laurence (2017). Erratum to: The presence of anaemia negatively influences survival in patients with POLG disease (Journal of Inherited Metabolic Disease, (2017), 40, 6, (861-866), 10.1007/s10545-017-0084-9). Journal of Inherited Metabolic Disease.  ISSN 0141-8955.  41(1), s 153- 153 . doi: 10.1007/s10545-017-0092-9
  • Rydning, Siri Lynne; Backe, Paul Hoff; Sousa, Mirta; Iqbal, Zafar; Øye, Ane-Marte; Sheng, Ying; Yang, Mingyi; Lin, Xiaolin; Slupphaug, Geir; Nordenmark, Tonje Haug; Vigeland, Magnus Dehli; Bjørås, Magnar; Tallaksen, Chantal & Selmer, Kaja Kristine (2017). Corrigendum: Novel UCHL1 mutations reveal new insights into ubiquitin processing. Human Molecular Genetics.  ISSN 0964-6906.  26(6), s 1217- 1218 . doi: 10.1093/hmg/ddx072
  • Tallaksen, Chantal & Müller, Ulrich (2017). Cancer and neurodegeneration: Time to move beyond Janus?. Neurology.  ISSN 0028-3878.  88(12), s 1106- 1107 . doi: 10.1212/WNL.0000000000003727
  • Arntzen, Kjell Arne; Høyer, Helle; Ingebrigtsen, Monica; Busk, Øyvind Løvold; Holla, Øystein Lunde; Tveten, Kristian; Hilmarsen, Hilde T; Ørstavik, Kristin; Tallaksen, Chantal; Nebuchennykh, Maria; Jonsrud, Christoffer; Braathen, Geir & Fagerheim, Toril (2016). Prevalence and spectrum of SH3TC2 mutations in Norway.
  • Gilhus, Nils Erik; Kerty, Emilia; Løseth, Sissel; Mygland, Åse & Tallaksen, Chantal (2016). Myasthenia gravis - diagnostikk og behandling. Tidsskrift for Den norske legeforening.  ISSN 0029-2001.  136(12/13), s 1089- 1094 . doi: 10.4045/tidsskr.15.1259
  • Jahic, Amir; ERICHSEN, ANNE KJERSTI; Deufel, Thomas; Tallaksen, Chantal & Beetz, Christian (2016). A polymorphic Alu insertion that mediates distinct disease-associated deletions. European Journal of Human Genetics.  ISSN 1018-4813.  24(9), s 1371- 1374 . doi: 10.1038/ejhg.2016.20
  • Horn, Morten Andreas; Retterstøl, Lars; Abdelnoor, Michael; Skjeldal, Ola & Tallaksen, Chantal (2015). Age-dependent penetrance among females with X-linked adrenoleukodystrophy. Brain.  ISSN 0006-8950.  138(1), s e325 . doi: 10.1093/brain/awu232
  • Du Montcel, Sophie Tezenas; Charles, Perrine; Goizet, Cyril; Marelli, Cecilia; Anheim, Mathieu; Guyant-Marchal, Lucie; Le Bayon, Alice; Vandenberghe, Nadia; Tchikviladze, Maia; Devos, David; Le Ber, Isabelle; N'Guyen, Karine; Cazeneuve, Cecile; Tallaksen, Chantal; Brice, Alexis & Durr, Alexandra (2012). Sample Size Estimation for Future Therapeutic Trials in SCAs. Neurology.  ISSN 0028-3878.  78
  • Wedding, Iselin Marie; Koht, Jeanette; Landro, N. I. & Tallaksen, Chantal (2012). Cerebellum - more than motor control? Cognition in spinocerebellar ataxia type 14. European Journal of Neurology.  ISSN 1351-5101.  19, s 62- 62
  • Maniaol, Angelina; Boldingh, Marion Ingeborg; Brunborg, Cathrine; Harbo, Hanne Flinstad & Tallaksen, Chantal (2011). A POPULATION-BASED DESCRIPTIVE EPIDEMIOLOGIC STUDY OF MYASTHENIA GRAVIS IN NORWAY. European Journal of Neurology.  ISSN 1351-5101.  18(S2), s 276- 276
  • Koht, Jeanette & Tallaksen, Chantal (2010). Two new autosomal dominant ataxia loci.
  • Tallaksen, Chantal & Coutinho, P (2010). Clinical diagnosis of hereditary spastic paraplegia. European Journal of Neurology.  ISSN 1351-5101.  17(supp. 3), s 642- 642
  • Tallaksen, Chantal & Reid, E. (2010). Molecular genetics of spastic paraplegia. European Journal of Neurology.  ISSN 1351-5101.  17, s 641- 641
  • ERICHSEN, ANNE KJERSTI; Koht, Jeanette Aimee; Abdelnoor, M & Tallaksen, Chantal (2008). Hereditary spastic paraplegia in south-eastern Norway. European Journal of Neurology.  ISSN 1351-5101.  15, s 354- 354

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Publisert 13. apr. 2011 11:45 - Sist endret 20. nov. 2015 11:35

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